Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
A |
T |
13: 60,992,152 (GRCm39) |
D291E |
probably benign |
Het |
Adamts15 |
A |
T |
9: 30,822,404 (GRCm39) |
|
probably null |
Het |
Adgrg7 |
A |
G |
16: 56,553,207 (GRCm39) |
I630T |
probably damaging |
Het |
Ahnak |
A |
G |
19: 8,980,569 (GRCm39) |
I618V |
probably benign |
Het |
Amotl2 |
T |
A |
9: 102,608,889 (GRCm39) |
V801E |
probably damaging |
Het |
Ankrd17 |
T |
C |
5: 90,430,779 (GRCm39) |
T1002A |
probably benign |
Het |
Bmp7 |
C |
T |
2: 172,711,998 (GRCm39) |
D409N |
probably damaging |
Het |
Bpifb2 |
A |
G |
2: 153,731,726 (GRCm39) |
N293S |
possibly damaging |
Het |
Ccdc162 |
A |
G |
10: 41,510,044 (GRCm39) |
C854R |
probably benign |
Het |
Ccdc171 |
A |
G |
4: 83,736,304 (GRCm39) |
E1225G |
probably damaging |
Het |
Cep350 |
T |
C |
1: 155,741,833 (GRCm39) |
E2146G |
possibly damaging |
Het |
Ces1a |
A |
C |
8: 93,771,469 (GRCm39) |
|
probably null |
Het |
Cfap45 |
T |
G |
1: 172,368,925 (GRCm39) |
D444E |
probably benign |
Het |
Cfap61 |
T |
C |
2: 145,843,802 (GRCm39) |
V296A |
probably benign |
Het |
Cgnl1 |
C |
T |
9: 71,552,931 (GRCm39) |
R1011H |
probably benign |
Het |
Cops4 |
C |
T |
5: 100,691,741 (GRCm39) |
R347C |
probably damaging |
Het |
D16Ertd472e |
G |
T |
16: 78,344,576 (GRCm39) |
D177E |
probably benign |
Het |
Dcdc2a |
T |
C |
13: 25,291,600 (GRCm39) |
V195A |
possibly damaging |
Het |
Dipk2a |
A |
G |
9: 94,419,436 (GRCm39) |
S165P |
probably damaging |
Het |
Dpagt1 |
G |
A |
9: 44,243,319 (GRCm39) |
V285I |
probably benign |
Het |
Dspp |
G |
T |
5: 104,323,552 (GRCm39) |
A232S |
probably damaging |
Het |
Efcab3 |
T |
C |
11: 104,615,411 (GRCm39) |
I726T |
possibly damaging |
Het |
Ephx2 |
G |
A |
14: 66,347,904 (GRCm39) |
|
|
Het |
Fat1 |
T |
C |
8: 45,405,511 (GRCm39) |
V754A |
possibly damaging |
Het |
Fstl3 |
G |
A |
10: 79,615,865 (GRCm39) |
C117Y |
probably damaging |
Het |
Gldc |
A |
T |
19: 30,077,314 (GRCm39) |
S953T |
possibly damaging |
Het |
Gm1123 |
T |
C |
9: 98,893,033 (GRCm39) |
N315S |
probably benign |
Het |
Golga2 |
A |
G |
2: 32,178,202 (GRCm39) |
E37G |
|
Het |
Gpr139 |
T |
A |
7: 118,743,835 (GRCm39) |
Q250L |
probably benign |
Het |
Grik3 |
C |
T |
4: 125,543,532 (GRCm39) |
R283C |
probably damaging |
Het |
Haao |
A |
C |
17: 84,154,081 (GRCm39) |
V22G |
probably damaging |
Het |
Hspg2 |
T |
A |
4: 137,266,490 (GRCm39) |
F1884I |
probably damaging |
Het |
Hyal3 |
G |
A |
9: 107,462,166 (GRCm39) |
G67S |
probably damaging |
Het |
Kbtbd3 |
T |
A |
9: 4,330,424 (GRCm39) |
I266K |
probably benign |
Het |
Klhl26 |
A |
C |
8: 70,905,499 (GRCm39) |
L137R |
probably damaging |
Het |
Krt15 |
A |
T |
11: 100,026,386 (GRCm39) |
V100E |
possibly damaging |
Het |
Lars1 |
A |
G |
18: 42,343,083 (GRCm39) |
|
probably null |
Het |
Lats1 |
C |
T |
10: 7,577,859 (GRCm39) |
Q328* |
probably null |
Het |
Lingo3 |
G |
A |
10: 80,670,463 (GRCm39) |
T489I |
probably damaging |
Het |
Lmtk2 |
T |
C |
5: 144,066,261 (GRCm39) |
V65A |
possibly damaging |
Het |
Lysmd1 |
T |
C |
3: 95,045,795 (GRCm39) |
S211P |
probably damaging |
Het |
Med15 |
C |
T |
16: 17,540,626 (GRCm39) |
S21N |
unknown |
Het |
Nav1 |
T |
C |
1: 135,512,656 (GRCm39) |
T135A |
probably benign |
Het |
Nt5c1a |
G |
C |
4: 123,102,272 (GRCm39) |
R66T |
probably benign |
Het |
Pclo |
T |
C |
5: 14,732,024 (GRCm39) |
Y3509H |
unknown |
Het |
Pkp4 |
G |
A |
2: 59,140,484 (GRCm39) |
G397R |
possibly damaging |
Het |
Ppp1r21 |
G |
A |
17: 88,856,958 (GRCm39) |
A138T |
probably benign |
Het |
Pum3 |
A |
T |
19: 27,401,642 (GRCm39) |
V136D |
probably benign |
Het |
Rab11fip3 |
A |
T |
17: 26,287,126 (GRCm39) |
D342E |
possibly damaging |
Het |
Rcvrn |
T |
A |
11: 67,590,883 (GRCm39) |
W156R |
probably damaging |
Het |
Rspry1 |
C |
T |
8: 95,349,813 (GRCm39) |
T67I |
probably benign |
Het |
Serpina1d |
T |
C |
12: 103,734,037 (GRCm39) |
D89G |
possibly damaging |
Het |
Sgsm3 |
T |
A |
15: 80,893,021 (GRCm39) |
V366E |
possibly damaging |
Het |
Shank3 |
T |
G |
15: 89,433,515 (GRCm39) |
L1420R |
probably benign |
Het |
Sirpb1b |
A |
T |
3: 15,608,100 (GRCm39) |
L215* |
probably null |
Het |
Slc16a13 |
C |
T |
11: 70,109,797 (GRCm39) |
V235I |
probably benign |
Het |
Slc16a14 |
T |
C |
1: 84,907,187 (GRCm39) |
D29G |
probably benign |
Het |
Speer1a |
T |
C |
5: 11,394,879 (GRCm39) |
V122A |
probably benign |
Het |
Spns2 |
T |
A |
11: 72,347,704 (GRCm39) |
T329S |
possibly damaging |
Het |
Sufu |
G |
A |
19: 46,439,108 (GRCm39) |
|
probably null |
Het |
Tll2 |
A |
G |
19: 41,108,608 (GRCm39) |
|
probably null |
Het |
Trim10 |
G |
A |
17: 37,180,773 (GRCm39) |
M1I |
probably null |
Het |
Trim42 |
A |
C |
9: 97,241,182 (GRCm39) |
N683K |
probably damaging |
Het |
Trmt5 |
A |
G |
12: 73,328,394 (GRCm39) |
S270P |
probably damaging |
Het |
Vmn1r59 |
C |
A |
7: 5,456,986 (GRCm39) |
R258L |
possibly damaging |
Het |
Vmn2r32 |
A |
G |
7: 7,482,851 (GRCm39) |
L41S |
probably benign |
Het |
Vmn2r93 |
A |
T |
17: 18,525,329 (GRCm39) |
E329V |
probably damaging |
Het |
Ywhae |
G |
T |
11: 75,655,487 (GRCm39) |
E253* |
probably null |
Het |
|
Other mutations in Abca9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00309:Abca9
|
APN |
11 |
110,051,342 (GRCm39) |
missense |
probably benign |
|
IGL00467:Abca9
|
APN |
11 |
110,036,496 (GRCm39) |
splice site |
probably benign |
|
IGL00886:Abca9
|
APN |
11 |
110,054,101 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01340:Abca9
|
APN |
11 |
110,021,453 (GRCm39) |
missense |
probably benign |
|
IGL01351:Abca9
|
APN |
11 |
110,039,729 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01383:Abca9
|
APN |
11 |
110,004,119 (GRCm39) |
splice site |
probably benign |
|
IGL01384:Abca9
|
APN |
11 |
110,036,463 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01482:Abca9
|
APN |
11 |
110,011,599 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01586:Abca9
|
APN |
11 |
110,045,243 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01589:Abca9
|
APN |
11 |
110,046,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01926:Abca9
|
APN |
11 |
110,026,155 (GRCm39) |
splice site |
probably benign |
|
IGL02059:Abca9
|
APN |
11 |
110,051,220 (GRCm39) |
splice site |
probably benign |
|
IGL02084:Abca9
|
APN |
11 |
110,021,423 (GRCm39) |
missense |
probably benign |
|
IGL02096:Abca9
|
APN |
11 |
110,056,806 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02096:Abca9
|
APN |
11 |
109,993,359 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02290:Abca9
|
APN |
11 |
110,026,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02303:Abca9
|
APN |
11 |
110,045,376 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02549:Abca9
|
APN |
11 |
109,992,879 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02687:Abca9
|
APN |
11 |
110,005,058 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02752:Abca9
|
APN |
11 |
110,018,194 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02814:Abca9
|
APN |
11 |
110,045,293 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02878:Abca9
|
APN |
11 |
110,029,155 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03088:Abca9
|
APN |
11 |
110,035,087 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03231:Abca9
|
APN |
11 |
110,046,094 (GRCm39) |
missense |
probably damaging |
0.96 |
R0050:Abca9
|
UTSW |
11 |
110,036,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0050:Abca9
|
UTSW |
11 |
110,036,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Abca9
|
UTSW |
11 |
110,035,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Abca9
|
UTSW |
11 |
110,035,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Abca9
|
UTSW |
11 |
110,036,405 (GRCm39) |
missense |
probably damaging |
0.99 |
R0189:Abca9
|
UTSW |
11 |
110,032,488 (GRCm39) |
splice site |
probably benign |
|
R0189:Abca9
|
UTSW |
11 |
109,999,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R0375:Abca9
|
UTSW |
11 |
110,006,273 (GRCm39) |
missense |
probably benign |
0.00 |
R0601:Abca9
|
UTSW |
11 |
110,007,884 (GRCm39) |
critical splice donor site |
probably null |
|
R0624:Abca9
|
UTSW |
11 |
110,030,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Abca9
|
UTSW |
11 |
110,042,889 (GRCm39) |
missense |
probably benign |
0.02 |
R1004:Abca9
|
UTSW |
11 |
110,042,780 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1222:Abca9
|
UTSW |
11 |
110,035,890 (GRCm39) |
splice site |
probably benign |
|
R1451:Abca9
|
UTSW |
11 |
110,018,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Abca9
|
UTSW |
11 |
110,051,342 (GRCm39) |
missense |
probably benign |
|
R1462:Abca9
|
UTSW |
11 |
110,051,342 (GRCm39) |
missense |
probably benign |
|
R1474:Abca9
|
UTSW |
11 |
110,036,405 (GRCm39) |
missense |
probably damaging |
0.99 |
R1499:Abca9
|
UTSW |
11 |
110,030,458 (GRCm39) |
missense |
probably benign |
0.00 |
R1778:Abca9
|
UTSW |
11 |
110,021,542 (GRCm39) |
nonsense |
probably null |
|
R2015:Abca9
|
UTSW |
11 |
110,022,672 (GRCm39) |
missense |
probably benign |
0.01 |
R2295:Abca9
|
UTSW |
11 |
110,039,729 (GRCm39) |
missense |
probably damaging |
0.99 |
R2303:Abca9
|
UTSW |
11 |
110,049,052 (GRCm39) |
missense |
probably benign |
0.01 |
R2403:Abca9
|
UTSW |
11 |
110,006,280 (GRCm39) |
missense |
probably benign |
0.16 |
R2886:Abca9
|
UTSW |
11 |
110,035,712 (GRCm39) |
splice site |
probably benign |
|
R3435:Abca9
|
UTSW |
11 |
110,045,256 (GRCm39) |
missense |
probably benign |
0.24 |
R3976:Abca9
|
UTSW |
11 |
110,039,615 (GRCm39) |
missense |
probably benign |
0.25 |
R4335:Abca9
|
UTSW |
11 |
110,042,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4411:Abca9
|
UTSW |
11 |
110,042,781 (GRCm39) |
missense |
probably benign |
0.00 |
R4613:Abca9
|
UTSW |
11 |
110,035,610 (GRCm39) |
missense |
probably benign |
0.26 |
R4690:Abca9
|
UTSW |
11 |
110,039,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R4720:Abca9
|
UTSW |
11 |
110,018,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4751:Abca9
|
UTSW |
11 |
110,021,396 (GRCm39) |
missense |
probably benign |
0.00 |
R4797:Abca9
|
UTSW |
11 |
110,008,945 (GRCm39) |
missense |
probably benign |
|
R4818:Abca9
|
UTSW |
11 |
110,045,980 (GRCm39) |
critical splice donor site |
probably null |
|
R4903:Abca9
|
UTSW |
11 |
110,037,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:Abca9
|
UTSW |
11 |
110,042,874 (GRCm39) |
missense |
probably benign |
0.43 |
R4977:Abca9
|
UTSW |
11 |
110,026,899 (GRCm39) |
missense |
probably benign |
0.00 |
R5019:Abca9
|
UTSW |
11 |
110,056,760 (GRCm39) |
missense |
probably benign |
|
R5079:Abca9
|
UTSW |
11 |
110,036,395 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5082:Abca9
|
UTSW |
11 |
110,022,694 (GRCm39) |
missense |
probably benign |
|
R5093:Abca9
|
UTSW |
11 |
110,032,358 (GRCm39) |
missense |
probably damaging |
0.98 |
R5212:Abca9
|
UTSW |
11 |
109,998,052 (GRCm39) |
missense |
probably benign |
0.02 |
R5350:Abca9
|
UTSW |
11 |
110,006,364 (GRCm39) |
missense |
probably benign |
|
R5368:Abca9
|
UTSW |
11 |
110,036,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R5432:Abca9
|
UTSW |
11 |
110,032,380 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5436:Abca9
|
UTSW |
11 |
110,025,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R5497:Abca9
|
UTSW |
11 |
110,021,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R5503:Abca9
|
UTSW |
11 |
110,032,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R5594:Abca9
|
UTSW |
11 |
110,035,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R5742:Abca9
|
UTSW |
11 |
110,051,243 (GRCm39) |
missense |
probably damaging |
0.98 |
R5776:Abca9
|
UTSW |
11 |
109,998,286 (GRCm39) |
splice site |
probably null |
|
R5781:Abca9
|
UTSW |
11 |
109,992,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Abca9
|
UTSW |
11 |
110,007,902 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5923:Abca9
|
UTSW |
11 |
110,051,378 (GRCm39) |
missense |
probably benign |
0.09 |
R6020:Abca9
|
UTSW |
11 |
110,036,439 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6179:Abca9
|
UTSW |
11 |
110,025,080 (GRCm39) |
missense |
probably benign |
0.05 |
R6245:Abca9
|
UTSW |
11 |
110,026,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R6249:Abca9
|
UTSW |
11 |
110,036,453 (GRCm39) |
missense |
probably benign |
|
R6365:Abca9
|
UTSW |
11 |
110,036,481 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6385:Abca9
|
UTSW |
11 |
110,025,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R6481:Abca9
|
UTSW |
11 |
110,056,788 (GRCm39) |
nonsense |
probably null |
|
R6675:Abca9
|
UTSW |
11 |
110,006,302 (GRCm39) |
missense |
probably benign |
|
R6909:Abca9
|
UTSW |
11 |
110,006,323 (GRCm39) |
missense |
probably benign |
0.01 |
R7429:Abca9
|
UTSW |
11 |
110,018,252 (GRCm39) |
frame shift |
probably null |
|
R7431:Abca9
|
UTSW |
11 |
110,018,252 (GRCm39) |
frame shift |
probably null |
|
R7621:Abca9
|
UTSW |
11 |
110,051,359 (GRCm39) |
missense |
probably benign |
0.00 |
R7623:Abca9
|
UTSW |
11 |
109,998,384 (GRCm39) |
missense |
probably benign |
0.27 |
R7660:Abca9
|
UTSW |
11 |
110,006,278 (GRCm39) |
missense |
probably benign |
|
R7784:Abca9
|
UTSW |
11 |
110,045,243 (GRCm39) |
nonsense |
probably null |
|
R7798:Abca9
|
UTSW |
11 |
110,029,005 (GRCm39) |
missense |
probably benign |
0.45 |
R7839:Abca9
|
UTSW |
11 |
110,025,085 (GRCm39) |
missense |
probably benign |
0.43 |
R7891:Abca9
|
UTSW |
11 |
110,054,098 (GRCm39) |
missense |
probably benign |
0.03 |
R7894:Abca9
|
UTSW |
11 |
109,997,415 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8030:Abca9
|
UTSW |
11 |
110,011,534 (GRCm39) |
missense |
probably benign |
|
R8133:Abca9
|
UTSW |
11 |
110,018,289 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8195:Abca9
|
UTSW |
11 |
110,029,155 (GRCm39) |
missense |
probably benign |
0.01 |
R8304:Abca9
|
UTSW |
11 |
109,997,954 (GRCm39) |
critical splice donor site |
probably null |
|
R8386:Abca9
|
UTSW |
11 |
110,021,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R8390:Abca9
|
UTSW |
11 |
110,036,456 (GRCm39) |
missense |
probably benign |
0.01 |
R8692:Abca9
|
UTSW |
11 |
110,032,409 (GRCm39) |
missense |
probably benign |
0.11 |
R8721:Abca9
|
UTSW |
11 |
110,035,115 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8738:Abca9
|
UTSW |
11 |
110,056,817 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R8900:Abca9
|
UTSW |
11 |
110,045,218 (GRCm39) |
missense |
probably benign |
|
R8948:Abca9
|
UTSW |
11 |
110,054,206 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8950:Abca9
|
UTSW |
11 |
110,054,206 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8964:Abca9
|
UTSW |
11 |
110,038,075 (GRCm39) |
nonsense |
probably null |
|
R9019:Abca9
|
UTSW |
11 |
110,011,522 (GRCm39) |
missense |
|
|
R9034:Abca9
|
UTSW |
11 |
110,039,615 (GRCm39) |
missense |
probably benign |
0.25 |
R9035:Abca9
|
UTSW |
11 |
110,021,461 (GRCm39) |
missense |
probably damaging |
0.97 |
R9086:Abca9
|
UTSW |
11 |
109,992,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R9199:Abca9
|
UTSW |
11 |
110,056,770 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9402:Abca9
|
UTSW |
11 |
110,049,154 (GRCm39) |
missense |
probably benign |
0.14 |
R9414:Abca9
|
UTSW |
11 |
110,035,100 (GRCm39) |
missense |
probably damaging |
0.97 |
R9554:Abca9
|
UTSW |
11 |
110,029,107 (GRCm39) |
missense |
probably benign |
|
R9626:Abca9
|
UTSW |
11 |
110,011,606 (GRCm39) |
missense |
probably benign |
0.01 |
R9651:Abca9
|
UTSW |
11 |
110,006,319 (GRCm39) |
missense |
probably benign |
0.09 |
R9665:Abca9
|
UTSW |
11 |
110,006,281 (GRCm39) |
missense |
probably benign |
0.00 |
R9665:Abca9
|
UTSW |
11 |
110,006,280 (GRCm39) |
missense |
probably benign |
|
R9731:Abca9
|
UTSW |
11 |
110,025,024 (GRCm39) |
missense |
probably benign |
|
Z1176:Abca9
|
UTSW |
11 |
110,026,201 (GRCm39) |
missense |
probably benign |
0.02 |
|